Добірка наукової літератури з теми "Aryl Compounds"
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Статті в журналах з теми "Aryl Compounds"
Wang, Xi-Cun, Fang Wang, Zheng-Jun Quan, Man-Gang Wang, and Zheng Li. "An efficient and clean synthesis of 1-aroyl-3-aryl-4-substituted imidazole-2-thiones in water." Journal of Chemical Research 2005, no. 11 (November 2005): 689–90. http://dx.doi.org/10.3184/030823405774909423.
Повний текст джерелаKrutošíková, Alžbeta, Miloslava Dandárová, and Juraj Alföldi. "5-Aryl-2-furancarbaldehyde Hydrazones and Related Compounds." Collection of Czechoslovak Chemical Communications 58, no. 8 (1993): 1905–13. http://dx.doi.org/10.1135/cccc19931905.
Повний текст джерелаSoni, Love Kumar, Tamanna Narsinghani, and Rica Jain. "Synthesis and Antibacterial Screening of Some 1-Aroyl-3-aryl Thiourea Derivatives." ISRN Medicinal Chemistry 2014 (January 29, 2014): 1–6. http://dx.doi.org/10.1155/2014/393102.
Повний текст джерелаKalam, Sirisha, Rajyalaxmi I, and Olivia S. "Synthesis and In vitro P-Glycoprotein Inhibitory Activity of Novel 1,4-Dihydropyridine Derivatives." International Journal of Pharmaceutical Sciences and Nanotechnology 7, no. 3 (August 31, 2014): 2544–52. http://dx.doi.org/10.37285/ijpsn.2014.7.3.6.
Повний текст джерелаRaval, J. P., and K. R. Desai. "Synthesis of 3-Phenyl-4[4-(m-nitrophenyl)-N-2-(2’-arylureido / arylthioureido-4’-N-morpholino-s-triazin)-benzo-[6,7]-coumarins and their Applicatiions." E-Journal of Chemistry 1, no. 5 (2004): 211–15. http://dx.doi.org/10.1155/2004/873425.
Повний текст джерелаKudalkar, Gaurav P., Virendra K. Tiwari, Joshua D. Lee, and David B. Berkowitz. "A Hammett Study of Clostridium acetobutylicum Alcohol Dehydrogenase (CaADH): An Enzyme with Remarkable Substrate Promiscuity and Utility for Organic Synthesis." Synlett 31, no. 03 (January 16, 2020): 237–47. http://dx.doi.org/10.1055/s-0039-1691576.
Повний текст джерелаChandra, Priyanka, Swastika Ganguly, Rajdeep Dey, and Biswatrish Sarkar. "Synthesis, antibacterial activities, binding mode analysis and predictive ADME studies of novel 1-(aryl)-2-(1H-imidazol-1-yl)methanones." INTERNATIONAL JOURNAL OF PHARMACEUTICAL EDUCATION AND RESEARCH (IJPER) 2, no. 02 (December 30, 2020): 39–45. http://dx.doi.org/10.37021/ijper.v2i2.2.
Повний текст джерелаChandra, Priyanka, Swastika Ganguly, Rajdeep Dey, and Biswatrish Sarkar. "Synthesis, antibacterial activities, binding mode analysis and predictive ADME studies of novel 1-(aryl)-2-(1H-imidazol-1-yl)methanones." INTERNATIONAL JOURNAL OF PHARMACEUTICAL EDUCATION AND RESEARCH (IJPER) 2, no. 02 (December 30, 2020): 39–45. http://dx.doi.org/10.37021/ijper.v2i2.2.
Повний текст джерелаWang, Lizhong, Zhenjie Su, Siran Qian, Weijian Ye, and Cunde Wang. "Efficient Preparation of 2,3-Disubstituted Cyclopropane-1-Carbonitriles via Selective Decarboxylation of 1-Cyanocyclopropane-1-Carboxylates." Journal of Chemical Research 41, no. 11 (November 2017): 636–40. http://dx.doi.org/10.3184/174751917x15094552081161.
Повний текст джерелаUtri, Gerhard, Karl-Eberhard Schwarzhans, and Günter M. Allmaier. "Ferrocenyl-aryl-plumbane / Ferrocenyl-aryl-plumbanes." Zeitschrift für Naturforschung B 45, no. 6 (June 1, 1990): 755–62. http://dx.doi.org/10.1515/znb-1990-0606.
Повний текст джерелаДисертації з теми "Aryl Compounds"
Leyva-Ramos, Elisa. "The temperature dependent photochemistry of aryl azides and aryl diazo compounds /." The Ohio State University, 1986. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487267024997622.
Повний текст джерелаLeary, Edmund. "Single Molecule Conductance of Dithiahexyl-Aryl Compounds." Thesis, University of Liverpool, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.507724.
Повний текст джерелаRoss, Jennifer Nicola. "Alkoxy- substituted aryl- and benzyl- organotin compounds." Thesis, University of Aberdeen, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.324880.
Повний текст джерелаKhashoqji, Moayad. "Structural characterisation of novel poly-aryl compounds." Thesis, University of Manchester, 2016. https://www.research.manchester.ac.uk/portal/en/theses/structural-characterisation-of-novel-polyaryl-compounds(3fb1fac6-548a-4afc-8ac2-5a14885b0ba4).html.
Повний текст джерелаRowland, Keith E. (Keith Edward). "An NMR Investigation of Aryl Mercury Compounds." Thesis, North Texas State University, 1987. https://digital.library.unt.edu/ark:/67531/metadc500453/.
Повний текст джерелаGuena, Thierry. "Electrochemistry of aryl carbonyl compounds in flow cells." Thesis, University of Southampton, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.243180.
Повний текст джерелаHeaton, Julie N. "Generation and reactions of aryl and alkyl thionitroso compounds." Thesis, Durham University, 1992. http://etheses.dur.ac.uk/6129/.
Повний текст джерелаAprahamian, Steve Lawrence. "Rearrangement-displacement of aryl(chloromethyl)diphenylsilanes with nucleophiles /." The Ohio State University, 1986. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487265555439529.
Повний текст джерелаAl-Harthy, Farida. "Separation of aryl nitro-compounds by HPLC on monolithic columns." Thesis, Loughborough University, 2009. https://dspace.lboro.ac.uk/2134/8683.
Повний текст джерелаNg, Fei-yeung, and 吳飛洋. "Structure and properties of self-assembled coordination compounds: homoleptic d10-metal aryl/alkylacetylides, ruthenium n-heterocyclesand picolinates." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2006. http://hub.hku.hk/bib/B37878566.
Повний текст джерелаКниги з теми "Aryl Compounds"
Chehimi, Mohamed M., Jean Pinson, and Fatima Mousli, eds. Aryl Diazonium Salts and Related Compounds. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-04398-7.
Повний текст джерелаElings, Jacob Antonius. Solid-acid catalysed reactions with epoxides and allyl aryl ethers. Delft, Netherlands: Delft University Press, 1997.
Знайти повний текст джерелаR, Williams John. Development and preliminary evaluation of aryl ester boundary additives for perfluoropolyethers. Cleveland, Ohio: National Aeronautics and Space Administration, Lewis Research Center, 1994.
Знайти повний текст джерелаInternational Conference on Carcinogenic and Mutagenic N-Substituted Aryl Compounds (3rd 1987 Dearborn, Mich.). Carcinogenic and mutagenic responses to aromatic amines and nitroarenes: Proceedings of the Third International Conference on Carcinogenic and Mutagenic N-Substituted Aryl Compounds, held April 25-28, 1987, in Dearborn Michigan. Edited by King Charles M. 1932-, Romano Louis James 1950-, and Schuetzle Dennis 1942-. New York: Elsevier, 1988.
Знайти повний текст джерелаPerry, Philip J. Synthesis and biological evaluation of novel cytotoxic heterocyclic compounds: Furo (2,3-b) naphthoquinones and 2-aryl-4H-3,1-benzoxazin-4-ones. Leicester: De Montfort University, 1996.
Знайти повний текст джерелаBaltrušis, Romualdas. Sintez, prevrashchenii︠a︡ i svoĭstva N-aril (geterot︠s︡iklil)-[beta]-alaninov: Monografii︠a︡. Kaunas: Tekhnologii︠a︡, 1999.
Знайти повний текст джерелаPohjanvirta, Raimo. The AH receptor in biology and toxicology. Hoboken, N.J: Wiley, 2011.
Знайти повний текст джерелаCarcinogenic and mutagenic N-substituted aryl compounds. [Research Triangle Park, NC]: National Institutes of Health, National Institute of Environmental Health Sciences, 1994.
Знайти повний текст джерелаMousli, Fatima, Mohamed Mehdi Chehimi, and Jean Pinson. Aryl Diazonium Salts and Related Compounds: Surface Chemistry and Applications. Springer International Publishing AG, 2022.
Знайти повний текст джерелаChehimi, Mohamed Mehdi. Aryl Diazonium Salts: New Coupling Agents in Polymer and Surface Science. Wiley & Sons, Incorporated, John, 2012.
Знайти повний текст джерелаЧастини книг з теми "Aryl Compounds"
McCreery, Richard, and Adam Johan Bergren. "Diazonium Compounds in Molecular Electronics." In Aryl Diazonium Salts, 219–39. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527650446.ch10.
Повний текст джерелаRappich, Jörg, Xin Zhang, and Karsten Hinrichs. "Electronic Properties of Si Surfaces Modified by Aryl Diazonium Compounds." In Aryl Diazonium Salts, 241–53. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527650446.ch11.
Повний текст джерелаSaad, Ahmed, and Marta Cerruti. "Diazonium Salts and Related Compounds for Biomedical Applications." In Aryl Diazonium Salts and Related Compounds, 263–85. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-04398-7_14.
Повний текст джерелаBélanger, Daniel. "Diazonium Salts and Related Compounds in Electrochemical Energy Storage and Conversion." In Aryl Diazonium Salts and Related Compounds, 427–51. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-04398-7_22.
Повний текст джерелаVieillard, Julien, Franck Le Derf, Charlène Gadroy, and Brahim Samir. "Modification and Uses of Synthetic and Biobased Polymeric Materials." In Aryl Diazonium Salts and Related Compounds, 195–209. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-04398-7_10.
Повний текст джерелаGuselnikova, Olga, Natalia S. Soldatova, and Pavel S. Postnikov. "Iodonium Salts as Reagents for Surface Modification: From Preparation to Reactivity in Surface-Assisted Transformations." In Aryl Diazonium Salts and Related Compounds, 79–96. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-04398-7_4.
Повний текст джерелаYagci, Yusuf, and Mohamed M. Chehimi. "Aryldiazonium Salts as Photoinitiators for Cationic and Free Radical Polymerizations." In Aryl Diazonium Salts and Related Compounds, 309–15. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-04398-7_16.
Повний текст джерелаRodríguez González, Miriam C., Kunal S. Mali, and Steven De Feyter. "Covalent Modification of Graphite and Graphene Using Diazonium Chemistry." In Aryl Diazonium Salts and Related Compounds, 157–81. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-04398-7_8.
Повний текст джерелаMousli, Fatima, Youssef Snoussi, Mohamed M. Chehimi, and Robert Wojcieszak. "On the Use of Diazonium Salts in the Design of Catalytic Hybrid Materials and Coatings." In Aryl Diazonium Salts and Related Compounds, 287–308. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-04398-7_15.
Повний текст джерелаVautrin-Ul, Christine. "Modification of sp2 Carbon Allotropes with Diazonium Salts—Focus on Carbon Nanotubes Functionalization." In Aryl Diazonium Salts and Related Compounds, 137–56. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-04398-7_7.
Повний текст джерелаТези доповідей конференцій з теми "Aryl Compounds"
Forostyanko, Anna, Elena Vasileva, and Irina Proskurina. "SYNTHESIS OF 5-(4’-NITROPHENYL)-3-ARYL-1,2,4-OXADIAZOLES." In Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m758.aks-2019/222-226.
Повний текст джерелаAndrić, Deana B., Slađana Dukić-Stefanovic, Jelena Z. Penjišević, Ivana I. Jevtić, Vladimir B. Šukalović, Relja Suručić, and Slađana Kostić-Rajačić. "DESIGN, SYNTHESIS AND PHARMACOLOGICAL EVALUATION OF NOVEL N- {4-[2-(4-ARYL-PIPERAZIN-1-YL)-ETHYL]-PHENYL}-ARYLAMIDES." In 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac, 2021. http://dx.doi.org/10.46793/iccbi21.355a.
Повний текст джерелаAnichina, K. "SYNTHESIS AND ANTINEMATODAL ACTIVITY STUDIES OF SOME FUSED TRIAZINOBENZIMIDAZOLES." In International Trends in Science and Technology. RS Global Sp. z O.O., 2020. http://dx.doi.org/10.31435/rsglobal_conf/30122020/7351.
Повний текст джерелаVasilenko, Dmitry, Kirill Sadovnikov, Arina Tukhbatullina та Elena Averina. "NOVEL REACTION OF HETEROCYCLIZATION OF β-ARYL SUBSTITUTED α,β-UNSATURATED KETONES. SYNTHESIS OF 4-NITROISOXAZOLES AND π-CONJUGATED ISOXAZOLE-BASED SYSTEMS WITH VALUABLE PHOTOPHYSICAL PROPARTIESE PHOTOPHYSICAL PROPARTIES". У Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m731.aks-2019/102-104.
Повний текст джерелаD., Chavan M., Karamthoti M. B., and Kurra S. B. "Screening of Antiseizure Activity of Aryl Acetic Acid Compounds in Wistar Albino Rats by using PTZ and MES Tests." In 20th Joint Annual Conference of Indian Epilepsy Society and Indian Epilepsy Association. Thieme Medical and Scientific Publishers Private Ltd., 2018. http://dx.doi.org/10.1055/s-0039-1694877.
Повний текст джерелаAparicio, Carmen Blanco, Julen Oyarzabal, Oliver Renner, Rosa Maria Alvarez, Sandra Peregrina, Ana Corrionero, Carl Gustaf Saluste, et al. "Abstract B227: Discovery of 3-aryl-3H-[1,2,3]triazolo[4,5-b]pyridin-5-ylamine compounds as potent, selective and orally bioavailable inhibitors of PIM kinases." In Abstracts: AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics--Nov 12-16, 2011; San Francisco, CA. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1535-7163.targ-11-b227.
Повний текст джерелаAparicio, Carmen Blanco, Sonia Martinez, Beatriz Garcia-Serelde, Ana Maria Garcia-Collazo, Nuria Ajenjo, Beatriz Noya, Ana Corrionero, et al. "Abstract B228: Discovery of 6-Methyl-3-aryl-7,8-dihydro-6H-9-oxa-1,2,3a,4,6-pentaaza-cyclopenta[a]naphthalen-5-ylamine compounds as Pim kinase inhibitors with potent activity in tumoral cell lines and special binding mode." In Abstracts: AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics--Nov 12-16, 2011; San Francisco, CA. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1535-7163.targ-11-b228.
Повний текст джерелаCline, Kjetil, Andrew LaFlam, Logan Smith, Margaret Nowicki, and Nicholas Ku. "Additive Manufacturing With Ceramics." In ASME 2020 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2020. http://dx.doi.org/10.1115/imece2020-23253.
Повний текст джерелаЗвіти організацій з теми "Aryl Compounds"
Jayatissa, Kuruppu. A Metal-Free Approach to Biaryl Compounds: Carbon-Carbon Bond Formation from Diaryliodonium Salts and Aryl Triolborates. Portland State University Library, January 2000. http://dx.doi.org/10.15760/etd.2226.
Повний текст джерела